BELLIS PERENNIS

Product NDC
15631-0077
Requested package NDC
15631-0077-1
11-digit product format
156310077
Labeler code
15631
Product ID
15631-0077_ccf8ef09-bce5-730e-e053-2995a90a74e3
Type
HUMAN OTC DRUG
Nonproprietary name
BELLIS PERENNIS
Dosage form
PELLET
Route
ORAL
Labeler
Rxhomeo Private Limited d.b.a. Rxhomeo, Inc
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2015-09-12
Substance
BELLIS PERENNIS
Active strength
1 [hp_X]/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 1 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2019-12-08 06:16 UTC · source 2019-12-05excluded packagepackage15631-007715631-0077-1EExcluded after deficient or non-compliant submission was not correctedexcluded / ndc_excluded.zip110d247fa046…a55b01930146…

Additional Listing Data#

Finished product
Yes
Brand name base
BELLIS PERENNIS
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BELLIS PERENNIS1 [hp_X]/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
2HU33I03UYInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
157ee323-d7f2-41f4-a941-580632487359Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
15631-0077-0BELLIS PERENNIS100 in 1 PACKAGEPELLET1003
15631-0077-1BELLIS PERENNIS200 in 1 PACKAGEPELLET2003
15631-0077-2BELLIS PERENNIS400 in 1 PACKAGEPELLET4003
15631-0077-3BELLIS PERENNIS750 in 1 PACKAGEPELLET7503
15631-0077-4BELLIS PERENNIS2500 in 1 PACKAGEPELLET25003
15631-0077-5BELLIS PERENNIS12500 in 1 PACKAGEPELLET125003
15631-0077-6BELLIS PERENNIS500 in 1 PACKAGEPELLET5003
15631-0077-7BELLIS PERENNIS1000 in 1 PACKAGEPELLET10003

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
BELLIS PERENNISACTIVE INGREDIENT2HU33I03UYBELLIS PERENNIS PELLET [RXHOMEO PRIVATE LIMITED D.B.A. RXHOMEO, INC]1
BELLIS PERENNISACTIVE MOIETY2HU33I03UYBELLIS PERENNIS PELLET [RXHOMEO PRIVATE LIMITED D.B.A. RXHOMEO, INC]1
SUCROSEINACTIVE INGREDIENTC151H8M554BELLIS PERENNIS PELLET [RXHOMEO PRIVATE LIMITED D.B.A. RXHOMEO, INC]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
15631-0077BELLIS PERENNIS PELLET [RXHOMEO PRIVATE LIMITED D.B.A. RXHOMEO, INC]3Current NDC, Legacy NDC, 8 package rows20210928_157ee323-d7f2-41f4-a941-580632487359.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
BELLIS PERENNISBELLIS PERENNISRxhomeo Private Limited d.b.a. Rxhomeo, Inc157ee323-d7f2-41f4-a941-5806324873592021-09-27WarningsExact identifier
ndc (package): 15631-0077-1
ndc (product): 15631-0077
ndc11 (package): 15631007701

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
15631-0077-115631007701200 PELLET in 1 PACKAGE (15631-0077-1) 200 pellet2018-01-010000-00-00NoNoCurrent